{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-04-01",
    "results": {
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      "status": "Terminated",
      "city": "Danvers",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
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      "recalling_firm": "Medtronic Vascular",
      "address_1": "35-37A Cherry Hill Drive",
      "address_2": "",
      "postal_code": "01923-2565",
      "voluntary_mandated": "Voluntary: Firm initiated",
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      "recall_number": "Z-1248-2021",
      "product_description": "Medtronic 6F Launcher Guide Catheter 100 cm EBU 3.0    Model Number: LA6EBU30",
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      "reason_for_recall": "Sterility may be compromised due to an unsealed pouch",
      "recall_initiation_date": "20210115",
      "center_classification_date": "20210311",
      "termination_date": "20230615",
      "report_date": "20210317",
      "code_info": "Lot Code: 220857555",
      "more_code_info": ""
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}